MEWIGEN runs a molecular genetic laboratory located in Dresden, a growing research hot spot in Germany. As our founders have their personal roots in genomic and tumor research themselves (see reference list), MEWIGEN provides a wide range of molecular genetic services related to human and tumor genetics for health care professionals successfully now for more than 10 years.

Our services include Sanger Sequencing of more than 600 genes of the human genome associated with hereditary diseases and of many more genes in diverse diagnostic panels by Next Generation Sequencing (NGS). Moreover, we offer cDNA analyses for the clarification of potential splice site mutations, fluorescence-based fragment length analyses (microsatellites, various trinucleotide repeat expansions such as Huntington’s and Ataxias) as well as analyses for gross genomic deletions and duplications and aberrant methylation of relevant sites. The range of our diagnostic spectrum is continuously expanded.